US7169778B2 - Pteridinones as kinase inhibitors - Google Patents

Pteridinones as kinase inhibitors Download PDF

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Publication number: US7169778B2
Authority: US; United States
Prior art keywords: amino; substituted; pteridin; phenyl; cyclopentyl
Prior art date: 1999-09-15
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Fee Related, expires 2020-10-24

Application number

US10/070,530

Other languages

English (en)

Other versions

US20030130286A1 (en

Inventor

William Alexander Denny

Gordon William Rewcastle

Ellen Dobrusin

James Bernard Kramer

Dennis Joseph McNamara

Howard Daniel Hollis Showalter

Peter Laurence Toogood

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Warner Lambert Co LLC

Original Assignee

Warner Lambert Co LLC

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1999-09-15

Filing date

2000-06-21

Publication date

2007-01-30

2000-06-21 Application filed by Warner Lambert Co LLC filed Critical Warner Lambert Co LLC

2000-06-21 Priority to US10/070,530 priority Critical patent/US7169778B2/en

2003-07-10 Publication of US20030130286A1 publication Critical patent/US20030130286A1/en

2006-10-27 Priority to US11/553,935 priority patent/US20070049600A1/en

2007-01-30 Application granted granted Critical

2007-01-30 Publication of US7169778B2 publication Critical patent/US7169778B2/en

2020-10-24 Adjusted expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

VWXIHLCLIOQWRA-UHFFFAOYSA-N 1h-pteridin-2-one Chemical class N1=CC=NC2=NC(O)=NC=C21 VWXIHLCLIOQWRA-UHFFFAOYSA-N 0.000 title 1
229940043355 kinase inhibitor Drugs 0.000 title 1
239000003757 phosphotransferase inhibitor Substances 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 149
125000000217 alkyl group Chemical group 0.000 claims abstract description 84
125000003545 alkoxy group Chemical group 0.000 claims abstract description 54
150000002367 halogens Chemical class 0.000 claims abstract description 51
229910052736 halogen Inorganic materials 0.000 claims abstract description 49
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 41
239000001257 hydrogen Substances 0.000 claims abstract description 40
125000002837 carbocyclic group Chemical group 0.000 claims abstract description 39
125000001072 heteroaryl group Chemical group 0.000 claims abstract description 37
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 35
229910052757 nitrogen Inorganic materials 0.000 claims abstract description 23
229910052760 oxygen Inorganic materials 0.000 claims abstract description 22
125000005842 heteroatom Chemical group 0.000 claims abstract description 21
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 18
239000001301 oxygen Substances 0.000 claims abstract description 18
125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 13
125000004446 heteroarylalkyl group Chemical group 0.000 claims abstract description 12
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 4
-1 phenoxy, hydroxy Chemical group 0.000 claims description 82
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 58
125000004663 dialkyl amino group Chemical group 0.000 claims description 49
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 47
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 45
125000003118 aryl group Chemical group 0.000 claims description 42
150000003839 salts Chemical class 0.000 claims description 35
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 29
125000000547 substituted alkyl group Chemical group 0.000 claims description 26
RGJOEKWQDUBAIZ-HDCXRZRFSA-N [[(2r,3s,4r,5r)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(3s)-3-hydroxy-2,2-dimethyl-4-oxo-4-[[3-oxo-3-(2-sulfanylethylamino)propyl]amino]butyl] hydrogen phosphate Chemical compound O[C@@H]1[C@H](OP(O)(O)=O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)(C)[C@H](O)C(=O)NCCC(=O)NCCS)O[C@H]1N1C2=NC=NC(N)=C2N=C1 RGJOEKWQDUBAIZ-HDCXRZRFSA-N 0.000 claims description 20
150000001733 carboxylic acid esters Chemical class 0.000 claims description 19
150000003857 carboxamides Chemical class 0.000 claims description 18
150000002825 nitriles Chemical class 0.000 claims description 17
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
125000004001 thioalkyl group Chemical group 0.000 claims description 17
150000003573 thiols Chemical class 0.000 claims description 17
125000005017 substituted alkenyl group Chemical group 0.000 claims description 16
125000000304 alkynyl group Chemical group 0.000 claims description 15
LJDZFAPLPVPTBD-UHFFFAOYSA-N nitroformic acid Chemical compound OC(=O)[N+]([O-])=O LJDZFAPLPVPTBD-UHFFFAOYSA-N 0.000 claims description 15
125000004426 substituted alkynyl group Chemical group 0.000 claims description 15
125000003342 alkenyl group Chemical group 0.000 claims description 14
125000004984 dialkylaminoalkoxy group Chemical group 0.000 claims description 13
150000001408 amides Chemical class 0.000 claims description 12
125000003282 alkyl amino group Chemical group 0.000 claims description 11
125000002431 aminoalkoxy group Chemical group 0.000 claims description 11
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 11
125000005236 alkanoylamino group Chemical group 0.000 claims description 9
125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims description 9
150000002148 esters Chemical class 0.000 claims description 9
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
125000002757 morpholinyl group Chemical group 0.000 claims description 9
125000004193 piperazinyl group Chemical group 0.000 claims description 9
125000003386 piperidinyl group Chemical group 0.000 claims description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
125000004103 aminoalkyl group Chemical group 0.000 claims description 8
239000008194 pharmaceutical composition Substances 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 8
125000000753 cycloalkyl group Chemical group 0.000 claims description 7
125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 6
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
PMVFPBHHPYGTOT-UHFFFAOYSA-N 6-(2,6-dichloro-3-hydroxyphenyl)-8-methyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound N=1C=C2N=C(C=3C(=C(O)C=CC=3Cl)Cl)C(=O)N(C)C2=NC=1NC(C=C1)=CC=C1N1CCOCC1 PMVFPBHHPYGTOT-UHFFFAOYSA-N 0.000 claims description 5
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 5
125000004414 alkyl thio group Chemical group 0.000 claims description 5
239000003085 diluting agent Substances 0.000 claims description 5
239000003937 drug carrier Substances 0.000 claims description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
125000006540 piperadinylalkyl group Chemical group 0.000 claims description 5
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 4
125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 4
125000001589 carboacyl group Chemical group 0.000 claims description 4
125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 4
239000000546 pharmaceutical excipient Substances 0.000 claims description 4
FPBMKRCNELOZRV-UHFFFAOYSA-N tert-butyl 4-[4-[(8-cyclopentyl-7-oxopteridin-2-yl)amino]phenyl]piperazine-1-carboxylate Chemical compound C1CN(C(=O)OC(C)(C)C)CCN1C(C=C1)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 FPBMKRCNELOZRV-UHFFFAOYSA-N 0.000 claims description 4
MOSSYTVPDMVLCJ-UHFFFAOYSA-N 2-(3-chloro-4-piperazin-1-ylanilino)-8-cyclopentylpteridin-7-one Chemical compound C=1C=C(N2CCNCC2)C(Cl)=CC=1NC(N=C12)=NC=C1N=CC(=O)N2C1CCCC1 MOSSYTVPDMVLCJ-UHFFFAOYSA-N 0.000 claims description 3
GWQLILGRIBWFTH-UHFFFAOYSA-N 2-[4-(3-aminopyrrolidin-1-yl)anilino]-8-cyclopentylpteridin-7-one Chemical compound C1C(N)CCN1C(C=C1)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 GWQLILGRIBWFTH-UHFFFAOYSA-N 0.000 claims description 3
TWLWOOPCEXYVBE-UHFFFAOYSA-N 5-fluoro-2-(6-fluoro-2-methylbenzimidazol-1-yl)-4-n-[4-(trifluoromethyl)phenyl]pyrimidine-4,6-diamine Chemical compound CC1=NC2=CC=C(F)C=C2N1C(N=1)=NC(N)=C(F)C=1NC1=CC=C(C(F)(F)F)C=C1 TWLWOOPCEXYVBE-UHFFFAOYSA-N 0.000 claims description 3
XKZVCLVXJAUEEE-UHFFFAOYSA-N 6-(2,6-dichlorophenyl)-8-methyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound N=1C=C2N=C(C=3C(=CC=CC=3Cl)Cl)C(=O)N(C)C2=NC=1NC(C=C1)=CC=C1N1CCOCC1 XKZVCLVXJAUEEE-UHFFFAOYSA-N 0.000 claims description 3
SFMVMYSZIILQHZ-UHFFFAOYSA-N 6-(3,5-dibromopyridin-4-yl)-8-methyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound N=1C=C2N=C(C=3C(=CN=CC=3Br)Br)C(=O)N(C)C2=NC=1NC(C=C1)=CC=C1N1CCOCC1 SFMVMYSZIILQHZ-UHFFFAOYSA-N 0.000 claims description 3
VTZRVCJFRVSILI-UHFFFAOYSA-N 6-(3,5-dichloro-2,6-dimethoxypyridin-4-yl)-2-[4-[2-(diethylamino)ethoxy]anilino]-8-methylpteridin-7-one Chemical compound C1=CC(OCCN(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C(=C(OC)N=C(OC)C=2Cl)Cl)C(=O)N2C)C2=N1 VTZRVCJFRVSILI-UHFFFAOYSA-N 0.000 claims description 3
JTWZNNWPAFJACJ-UHFFFAOYSA-N 6-(3,5-dichloro-2,6-dimethoxypyridin-4-yl)-8-methyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound COC1=NC(OC)=C(Cl)C(C=2C(N(C)C3=NC(NC=4C=CC(=CC=4)N4CCOCC4)=NC=C3N=2)=O)=C1Cl JTWZNNWPAFJACJ-UHFFFAOYSA-N 0.000 claims description 3
KGGZHEZJFLMSOJ-UHFFFAOYSA-N 6-(3,5-dichloropyridin-4-yl)-8-methyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound N=1C=C2N=C(C=3C(=CN=CC=3Cl)Cl)C(=O)N(C)C2=NC=1NC(C=C1)=CC=C1N1CCOCC1 KGGZHEZJFLMSOJ-UHFFFAOYSA-N 0.000 claims description 3
ASIIYBZDAMLQSS-UHFFFAOYSA-N 6-(3,5-dimethoxyphenyl)-8-ethyl-2-(pyridin-4-ylamino)pteridin-7-one Chemical compound N=1C=C2N=C(C=3C=C(OC)C=C(OC)C=3)C(=O)N(CC)C2=NC=1NC1=CC=NC=C1 ASIIYBZDAMLQSS-UHFFFAOYSA-N 0.000 claims description 3
FHADSBHFOMZHRE-UHFFFAOYSA-N 8-cyclopentyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound N1=C2N(C3CCCC3)C(=O)C=NC2=CN=C1NC(C=C1)=CC=C1N1CCOCC1 FHADSBHFOMZHRE-UHFFFAOYSA-N 0.000 claims description 3
BYJLIXXRIFPQTH-UHFFFAOYSA-N 8-cyclopentyl-2-(4-piperazin-1-ylanilino)pteridin-7-one Chemical compound N1=C2N(C3CCCC3)C(=O)C=NC2=CN=C1NC(C=C1)=CC=C1N1CCNCC1 BYJLIXXRIFPQTH-UHFFFAOYSA-N 0.000 claims description 3
OTCSXNHFLPNXHW-UHFFFAOYSA-N 8-cyclopentyl-2-(pyridin-4-ylamino)pteridin-7-one Chemical compound N1=C2N(C3CCCC3)C(=O)C=NC2=CN=C1NC1=CC=NC=C1 OTCSXNHFLPNXHW-UHFFFAOYSA-N 0.000 claims description 3
IKXHGNCGYSIJLT-UHFFFAOYSA-N 8-cyclopentyl-2-[4-(4-methylpiperazin-1-yl)anilino]pteridin-7-one Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 IKXHGNCGYSIJLT-UHFFFAOYSA-N 0.000 claims description 3
LTFJUFBZDRKWAI-UHFFFAOYSA-N 8-cyclopentyl-6-methyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound N1=C2N(C3CCCC3)C(=O)C(C)=NC2=CN=C1NC(C=C1)=CC=C1N1CCOCC1 LTFJUFBZDRKWAI-UHFFFAOYSA-N 0.000 claims description 3
JVTTYXFLKZSRJH-UHFFFAOYSA-N 8-cyclopentyl-6-methyl-2-[4-(4-methylpiperazin-1-yl)anilino]pteridin-7-one Chemical compound C1CN(C)CCN1C(C=C1)=CC=C1NC1=NC=C(N=C(C)C(=O)N2C3CCCC3)C2=N1 JVTTYXFLKZSRJH-UHFFFAOYSA-N 0.000 claims description 3
125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 3
125000005865 C2-C10alkynyl group Chemical group 0.000 claims description 3
125000003418 alkyl amino alkoxy group Chemical group 0.000 claims description 3
125000004093 cyano group Chemical group *C#N 0.000 claims description 3
125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 3
IZPQUQNXEKOJHD-UHFFFAOYSA-N n-[1-[4-[(8-cyclopentyl-7-oxopteridin-2-yl)amino]phenyl]pyrrolidin-3-yl]-3,3-dimethylbutanamide Chemical compound C1C(NC(=O)CC(C)(C)C)CCN1C(C=C1)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 IZPQUQNXEKOJHD-UHFFFAOYSA-N 0.000 claims description 3
125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 3
PACFJVOTNZCCMS-UHFFFAOYSA-N tert-butyl n-[1-[4-[(8-cyclopentyl-7-oxopteridin-2-yl)amino]phenyl]pyrrolidin-3-yl]carbamate Chemical compound C1C(NC(=O)OC(C)(C)C)CCN1C(C=C1)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 PACFJVOTNZCCMS-UHFFFAOYSA-N 0.000 claims description 3
IYNMEUFWCCKCDP-UHFFFAOYSA-N 2-(3-chloro-4-fluoroanilino)-8-cyclopentylpteridin-7-one Chemical compound C1=C(Cl)C(F)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 IYNMEUFWCCKCDP-UHFFFAOYSA-N 0.000 claims description 2
NTFVGDRIVOBXGC-UHFFFAOYSA-N 2-[3-chloro-4-(3-chloropyrrolidin-1-yl)anilino]-8-cyclopentylpteridin-7-one Chemical compound C1C(Cl)CCN1C(C(=C1)Cl)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 NTFVGDRIVOBXGC-UHFFFAOYSA-N 0.000 claims description 2
JFRQYWUUGCZUSX-UHFFFAOYSA-N 2-[3-chloro-4-[3-chloro-4-(trifluoromethyl)pyrrolidin-1-yl]anilino]-8-cyclopentylpteridin-7-one Chemical compound C1C(Cl)C(C(F)(F)F)CN1C(C(=C1)Cl)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 JFRQYWUUGCZUSX-UHFFFAOYSA-N 0.000 claims description 2
QCQJYBVMUSWCLF-UHFFFAOYSA-N 2-[4-(3-aminocyclopentanecarbonyl)anilino]-8-cyclopentylpteridin-7-one Chemical compound C1C(N)CCC1C(=O)C(C=C1)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 QCQJYBVMUSWCLF-UHFFFAOYSA-N 0.000 claims description 2
DDIKGEFRJASUNV-UHFFFAOYSA-N 2-[4-[2-(diethylamino)ethoxy]anilino]-6-(3,5-dimethoxyphenyl)-8-ethylpteridin-7-one Chemical compound C1=CC(OCCN(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C=C(OC)C=C(OC)C=2)C(=O)N2CC)C2=N1 DDIKGEFRJASUNV-UHFFFAOYSA-N 0.000 claims description 2
OZMUSTCAXPHENL-UHFFFAOYSA-N 2-[4-[2-(diethylamino)ethoxy]anilino]-8-methyl-6-phenylpteridin-7-one Chemical compound C1=CC(OCCN(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C=CC=CC=2)C(=O)N2C)C2=N1 OZMUSTCAXPHENL-UHFFFAOYSA-N 0.000 claims description 2
YZDQWJHDAXVFPA-UHFFFAOYSA-N 2-[4-[3-(2-aminopropan-2-yl)pyrrolidin-1-yl]-3-chloroanilino]-8-cyclopentylpteridin-7-one Chemical compound C1C(C(C)(N)C)CCN1C(C(=C1)Cl)=CC=C1NC1=NC=C(N=CC(=O)N2C3CCCC3)C2=N1 YZDQWJHDAXVFPA-UHFFFAOYSA-N 0.000 claims description 2
YVAMJXLFGYVFNQ-UHFFFAOYSA-N 4-[[6-(2,6-dichlorophenyl)-8-methyl-7-oxopteridin-2-yl]amino]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C(=CC=CC=2Cl)Cl)C(=O)N2C)C2=N1 YVAMJXLFGYVFNQ-UHFFFAOYSA-N 0.000 claims description 2
BRFNADVHVKIRKP-UHFFFAOYSA-N 4-[[6-(3,5-dichloro-2,6-dimethoxypyridin-4-yl)-8-methyl-7-oxopteridin-2-yl]amino]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C(=C(OC)N=C(OC)C=2Cl)Cl)C(=O)N2C)C2=N1 BRFNADVHVKIRKP-UHFFFAOYSA-N 0.000 claims description 2
XTFXYOOJMPYHGN-UHFFFAOYSA-N 4-[[6-(3,5-dichloropyridin-4-yl)-8-methyl-7-oxopteridin-2-yl]amino]-n,n-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C(=CN=CC=2Cl)Cl)C(=O)N2C)C2=N1 XTFXYOOJMPYHGN-UHFFFAOYSA-N 0.000 claims description 2
XDYSEPCCXCCKCB-UHFFFAOYSA-N 6-(2,6-dichlorophenyl)-2-[4-[2-(diethylamino)ethoxy]anilino]-8-methylpteridin-7-one Chemical compound C1=CC(OCCN(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C(=CC=CC=2Cl)Cl)C(=O)N2C)C2=N1 XDYSEPCCXCCKCB-UHFFFAOYSA-N 0.000 claims description 2
BKBUIGURKIBNQN-UHFFFAOYSA-N 6-(3,5-dichloropyridin-4-yl)-2-[4-[2-(diethylamino)ethoxy]anilino]-8-methylpteridin-7-one Chemical compound C1=CC(OCCN(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C(=CN=CC=2Cl)Cl)C(=O)N2C)C2=N1 BKBUIGURKIBNQN-UHFFFAOYSA-N 0.000 claims description 2
ZSUTVDRHBZDMKT-UHFFFAOYSA-N 8-cyclopentyl-2-(4-fluoro-3-methylanilino)-6-methylpteridin-7-one Chemical compound C1=C(F)C(C)=CC(NC=2N=C3N(C4CCCC4)C(=O)C(C)=NC3=CN=2)=C1 ZSUTVDRHBZDMKT-UHFFFAOYSA-N 0.000 claims description 2
WPKSQIGQEAHERC-UHFFFAOYSA-N 8-cyclopentyl-2-(4-fluoro-3-methylanilino)pteridin-7-one Chemical compound C1=C(F)C(C)=CC(NC=2N=C3N(C4CCCC4)C(=O)C=NC3=CN=2)=C1 WPKSQIGQEAHERC-UHFFFAOYSA-N 0.000 claims description 2
GFOFFJQPWPOVQO-UHFFFAOYSA-N 8-cyclopentyl-2-[4-[4-(3-piperazin-1-ylpropyl)piperidin-1-yl]anilino]pteridin-7-one Chemical compound N1=C2N(C3CCCC3)C(=O)C=NC2=CN=C1NC(C=C1)=CC=C1N(CC1)CCC1CCCN1CCNCC1 GFOFFJQPWPOVQO-UHFFFAOYSA-N 0.000 claims description 2
BOTIHYDKMILPFU-UHFFFAOYSA-N 8-cyclopentyl-2-[4-[4-[3-(2h-tetrazol-5-yl)propyl]piperidin-1-yl]anilino]pteridin-7-one Chemical compound N1=C2N(C3CCCC3)C(=O)C=NC2=CN=C1NC(C=C1)=CC=C1N(CC1)CCC1CCCC1=NN=NN1 BOTIHYDKMILPFU-UHFFFAOYSA-N 0.000 claims description 2
GEYIKMNUUVRSPH-UHFFFAOYSA-N n,n-diethyl-4-[(8-methyl-7-oxo-6-phenylpteridin-2-yl)amino]benzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1NC1=NC=C(N=C(C=2C=CC=CC=2)C(=O)N2C)C2=N1 GEYIKMNUUVRSPH-UHFFFAOYSA-N 0.000 claims description 2
RNSWQYQBRGOKMV-UHFFFAOYSA-N n-[4-[(8-cyclopentyl-6-methyl-7-oxopteridin-2-yl)amino]phenyl]propanamide Chemical compound C1=CC(NC(=O)CC)=CC=C1NC1=NC=C(N=C(C)C(=O)N2C3CCCC3)C2=N1 RNSWQYQBRGOKMV-UHFFFAOYSA-N 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims 12
YQYPLGPPOZBEJU-UHFFFAOYSA-N acetyloxycarbamic acid Chemical class CC(=O)ONC(O)=O YQYPLGPPOZBEJU-UHFFFAOYSA-N 0.000 claims 2
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 2
FXCKJOKRNXKDDL-UHFFFAOYSA-N 4-[(8-cyclopentyl-6-methyl-7-oxopteridin-2-yl)amino]benzenesulfonamide Chemical compound N1=C2N(C3CCCC3)C(=O)C(C)=NC2=CN=C1NC1=CC=C(S(N)(=O)=O)C=C1 FXCKJOKRNXKDDL-UHFFFAOYSA-N 0.000 claims 1
QDBOEKJCIQAAQP-UHFFFAOYSA-N 5-[(8-cyclopentyl-7-oxopteridin-2-yl)amino]-2-methylisoindole-1,3-dione Chemical compound C1=C2C(=O)N(C)C(=O)C2=CC=C1NC(N=C12)=NC=C1N=CC(=O)N2C1CCCC1 QDBOEKJCIQAAQP-UHFFFAOYSA-N 0.000 claims 1
AAGCLPSNCFMSER-UHFFFAOYSA-N 6-(2,6-dichloro-3-methoxyphenyl)-8-methyl-2-(4-morpholin-4-ylanilino)pteridin-7-one Chemical compound COC1=CC=C(Cl)C(C=2C(N(C)C3=NC(NC=4C=CC(=CC=4)N4CCOCC4)=NC=C3N=2)=O)=C1Cl AAGCLPSNCFMSER-UHFFFAOYSA-N 0.000 claims 1
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125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
210000004881 tumor cell Anatomy 0.000 description 1
231100000588 tumorigenic Toxicity 0.000 description 1
230000000381 tumorigenic effect Effects 0.000 description 1
125000001493 tyrosinyl group Chemical group [H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])(N([H])[H])C(*)=O 0.000 description 1
208000010576 undifferentiated carcinoma Diseases 0.000 description 1
229940070710 valerate Drugs 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011345 viscous material Substances 0.000 description 1
238000005303 weighing Methods 0.000 description 1
239000003871 white petrolatum Substances 0.000 description 1
229910000166 zirconium phosphate Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D475/00—Heterocyclic compounds containing pteridine ring systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D475/00—Heterocyclic compounds containing pteridine ring systems
- C07D475/02—Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4
- C07D475/04—Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4 with a nitrogen atom directly attached in position 2
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
- A—HUMAN NECESSITIES
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- A61P19/00—Drugs for skeletal disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Definitions

This invention relates to 8H-pteridine-7-ones, tetrahydropteridin-7-ones, 5H,8H-pteridine-6,7-diones and pteridine-7-ureas that inhibit cyclin-dependent serine/threonine kinase, Wee 1 tyrosine kinase, and growth factor-mediated tyrosine kinase enzymes, and as such are useful to treat cell proliferation diseases and disorders.
tyrosine kinases are a class of enzymes that catalyze the transfer of the terminal phosphate of adenosine triphosphate (ATP) to tyrosine residues on protein substrates.
Tyrosine kinases are essential for the propagation of growth factor signal transduction leading to cell cycle progression, cellular proliferation, differentiation, and migration.
Tyrosine kinases include cell surface growth factor receptor tyrosine kinases such as FGFr and PDGFr; as well as nonreceptor tyrosine kinases, including c-src and lck. Inhibition of these enzymes have been demonstrated to cause antitumor and antiangiogenesis activity (Hamby, et al., Pharmacol. Ther., 1999;82(2–3):169–193).
alkoxy straight or branched chain alkoxy groups having 1 to 10 carbon atoms, preferably 1–6 carbon atoms bonded through an oxygen atom, such as, for example, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, pentoxy, 2-pentyloxy, isopentoxy, neopentoxy, hexoxy, 2-hexoxy, 3-hexoxy, and 3-methylpentoxy.
These alkoxy groups may be substituted, for example with amino, alkylamino, and dialkylamino groups. Examples include aminomethoxy, 2-(methylamino)ethoxy, and 4-(dimethylamino)butoxy.
halogen in the present invention is meant fluorine, bromine, chlorine, and iodine.
compound 51 shown in Table 1 is named as 6-(2,6-dichloro-3-hydroxyphenyl)-8-methyl-2[[4-(morpholin-4-yl)phenyl]amino]-8H-pteridine-7-one.
Additional preferred compounds include the following:
the compounds of the present invention can exist in unsolvated forms as well as solvated forms, including hydrated forms.
the solvated forms, including hydrated forms are equivalent to unsolvated forms and are intended to be encompassed within the scope of the present invention.
the base addition salts of acidic compounds are prepared by contacting the free acid form with a sufficient amount of the desired base to produce the salt in the conventional manner.
the free acid form may be regenerated by contacting the salt form with an acid and isolating the free acid in a conventional manner.
the free acid forms differ from their respective salt forms somewhat in certain physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free acid for purposes of the present invention.
the compounds of the present invention are also useful research tools for studying the mechanism of action of those kinases, both in vitro and in vivo.
a typical active ingredient is 6-(3,4-diethoxyphenyl)-2-[4-(2-diethylaminoethoxy)-phenylamino]-8-n-butyl-8H-pteridin-7-one.
the composition is administered from 2 to 4 times a day for treatment of postsurgical restenosis.
a typical active ingredient utilized in the above preparation is the compound of Example 6 (7). This formulation is well-suited for prevention and treatment of psoriasis.

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US10/070,530 1999-09-15 2000-06-21 Pteridinones as kinase inhibitors Expired - Fee Related US7169778B2 (en)

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US10/070,530 US7169778B2 (en)	1999-09-15	2000-06-21	Pteridinones as kinase inhibitors
US11/553,935 US20070049600A1 (en)	1999-09-15	2006-10-27	Pteridinones as kinase inhibitors

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Application Number	Priority Date	Filing Date	Title
US15409599P	1999-09-15	1999-09-15
US60154095		1999-09-15
US10/070,530 US7169778B2 (en)	1999-09-15	2000-06-21	Pteridinones as kinase inhibitors
PCT/US2000/017037 WO2001019825A1 (en)	1999-09-15	2000-06-21	Pteridinones as kinase inhibitors

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OA12010A (en)	2006-04-19
CR6586A (es)	2004-02-02
IS6298A (is)	2002-03-13
AU5629500A (en)	2001-04-17
MA26819A1 (fr)	2004-12-20
US20030130286A1 (en)	2003-07-10
EA005287B1 (ru)	2004-12-30
NZ516872A (en)	2003-10-31
JP2003509425A (ja)	2003-03-11
HUP0202713A2 (hu)	2002-12-28
CA2393896A1 (en)	2001-03-22
WO2001019825A1 (en)	2001-03-22
NO20021239L (no)	2002-03-13
AU777468B2 (en)	2004-10-21
BR0013952A (pt)	2002-05-14
MXPA02001108A (es)	2002-08-20
IL148614A0 (en)	2002-09-12
EA200200078A1 (ru)	2002-12-26
SK3542002A3 (en)	2003-04-01
US20070049600A1 (en)	2007-03-01
BG106594A (en)	2002-12-29
EE200200140A (et)	2003-04-15
CZ2002846A3 (cs)	2003-02-12
HK1048992A1 (zh)	2003-04-25
AP2002002479A0 (en)	2002-06-30
NO20021239D0 (no)	2002-03-13
YU18502A (sh)	2004-12-31
EP1409487A1 (en)	2004-04-21
DZ3186A1 (fr)	2001-03-22
ZA200200896B (en)	2003-07-30
PL353269A1 (en)	2003-11-03
KR20020027649A (ko)	2002-04-13
CN1373763A (zh)	2002-10-09
HUP0202713A3 (en)	2005-02-28

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